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5-HT 受体影响轮状病毒引起的运动。

The 5-HT Receptor Affects Rotavirus-Induced Motility.

机构信息

Division of Molecular Medicine and Virology, Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Division of Infectious Diseases, Department of Medicine, Karolinska Institute, Stockholm, Sweden.

出版信息

J Virol. 2021 Jul 12;95(15):e0075121. doi: 10.1128/JVI.00751-21.

Abstract

Rotavirus infection is highly prevalent in children, and the most severe effects are diarrhea and vomiting. It is well accepted that the enteric nervous system (ENS) is activated and plays an important role, but knowledge of how rotavirus activates nerves within ENS and to the vomiting center is lacking. Serotonin is released during rotavirus infection, and antagonists to the serotonin receptor subtype 3 (5-HT receptor) can attenuate rotavirus-induced diarrhea. In this study, we used a 5-HT receptor knockout (KO) mouse model to investigate the role of this receptor in rotavirus-induced diarrhea, motility, electrolyte secretion, inflammatory response, and vomiting reflex. The number of diarrhea days ( = 0.03) and the number of mice with diarrhea were lower in infected 5-HT receptor KO than wild-type pups. investigation of fluorescein isothiocyanate (FITC)-dextran transit time showed that intestinal motility was lower in the infected 5-HT receptor KO compared to wild-type mice ( = 0.0023). Ussing chamber measurements of potential difference across the intestinal epithelia showed no significant difference in electrolyte secretion between the two groups. Immediate early gene cFos expression level showed no difference in activation of the vomiting center in the brain. Cytokine analysis of the intestine indicated a low effect of inflammatory response in rotavirus-infected mice lacking the 5-HT receptor. Our findings indicate that the 5-HT receptor is involved in rotavirus-induced diarrhea via its effect on intestinal motility and that the vagus nerve signaling to the vomiting center occurs also in the absence of the 5-HT receptor. The mechanisms underlying rotavirus-induced diarrhea and vomiting are not yet fully understood. To better understand rotavirus pathophysiology, characterization of nerve signaling within the ENS and through vagal efferent nerves to the brain, which have been shown to be of great importance to the disease, is necessary. Serotonin (5-HT), a mediator of both diarrhea and vomiting, has been shown to be released from enterochromaffin cells in response to rotavirus infection and the rotavirus enterotoxin NSP4. Here, we investigated the role of the serotonin receptor 5-HT, which is known to be involved in the nerve signals that regulate gut motility, intestinal secretion, and signal transduction through the vagus nerve to the brain. We show that the 5-HT receptor is involved in rotavirus-induced diarrhea by promoting intestinal motility. The findings shed light on new treatment possibilities for rotavirus diarrhea.

摘要

轮状病毒感染在儿童中非常普遍,其最严重的影响是腹泻和呕吐。众所周知,肠神经系统(ENS)被激活并发挥着重要作用,但轮状病毒如何激活 ENS 中的神经以及呕吐中枢的神经机制尚不清楚。轮状病毒感染时会释放血清素,而 5-羟色胺受体 3(5-HT 受体)拮抗剂可以减轻轮状病毒引起的腹泻。在这项研究中,我们使用 5-HT 受体敲除(KO)小鼠模型来研究该受体在轮状病毒诱导的腹泻、运动、电解质分泌、炎症反应和呕吐反射中的作用。与野生型幼鼠相比,感染 5-HT 受体 KO 的幼鼠腹泻天数( = 0.03)和腹泻幼鼠数量更少。用荧光素异硫氰酸酯(FITC)-葡聚糖转运时间的研究表明,感染 5-HT 受体 KO 的幼鼠的肠道运动低于野生型幼鼠( = 0.0023)。Ussing 室测量肠上皮层的跨膜电位差表明,两组之间的电解质分泌没有显著差异。呕吐中枢的即时早期基因 cFos 表达水平表明,在缺乏 5-HT 受体的轮状病毒感染小鼠中,呕吐中枢的激活没有差异。肠道细胞因子分析表明,缺乏 5-HT 受体的轮状病毒感染小鼠的炎症反应影响较小。我们的研究结果表明,5-HT 受体通过影响肠道运动参与轮状病毒诱导的腹泻,并且迷走神经信号传递到呕吐中枢也发生在缺乏 5-HT 受体的情况下。轮状病毒引起的腹泻和呕吐的机制尚未完全阐明。为了更好地了解轮状病毒的发病机制,有必要对 ENS 内的神经信号以及通过迷走神经传出神经传递到大脑的神经信号进行描述,这些信号对疾病的发生具有重要意义。血清素(5-HT)是腹泻和呕吐的介质,已被证明在轮状病毒感染和轮状病毒肠毒素 NSP4 后从肠嗜铬细胞中释放出来。在这里,我们研究了 5-HT 受体的作用,5-HT 受体已知参与调节肠道运动、肠道分泌以及通过迷走神经向大脑传递信号的神经信号。我们发现 5-HT 受体通过促进肠道运动参与轮状病毒诱导的腹泻。这些发现为轮状病毒腹泻的新治疗方法提供了思路。

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